Establishment registration
Arthrex Australia Pty Ltd.
FDA establishment registration 3019269298 · Frenchs Forest New South Wales, AU
Key facts
| Registration number | 3019269298 |
|---|---|
| Establishment name | Arthrex Australia Pty Ltd. |
| Owner/operator | ARTHREX, INC. |
| Owner/operator number | 1220287 |
| FEI number | 3019269298 |
| Address | Suite 501, 20 Rodborough Road |
| City | Frenchs Forest New South Wales |
| Country | AU |
| Registration valid through | 2026 |
| Product codes listed | BWN, DXJ, EBW, EQH, FMF, FMP, FSM, FWB, FWZ, FZW, GAB, GAP, GAT, GAZ, GCJ, GEI, GFA, GFF, HIF, HRS, HRX, HSB, HSD, HST, HTC, HTD, HTJ, HTN, HTO, HTW and 33 more |
| Device classes | 1, 2 |
At a glance
- 100–999 Device listings
- 1,000+ UDI devices (GUDID)
- Current Registration current
- None FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database